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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1167생성일: 2026년 10월 23일

6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamine → 6-Chloropyrimidine-2,4,5-triamine

https://huagongshe.com/ko/reaction/1167

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamineHCID 267764—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물6-Chloropyrimidine-2,4,5-triamineHCID 50050575.7%

반응 단계

A suspension of 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine (24.55 g, 0.0906 mol) in ethanol (640 ml), water (640 ml) and acetic acid (64 ml) was heated to 70° under nitrogen. Zinc dust (75 g) was added slowly over 1 hour, and then the reaction was stirred an additional hour at 70°. Then the reaction was cooled to room temperature and filtered under nitrogen. The filtrate was cooled to 0° and the pH was raised to 10 with 10% sodium hydroxide (400 ml). The precipitated zinc hydroxide was removed by filtration through Celite, and the dark red filtrate was neutralized to pH 7 with glacial acetic acid and concentrated to 300 ml. Water (50 ml) was added, the reaction was cooled to 0°, and the pH raised to 9 with 10% NaOH. The solution was allowed to stand at 5° for 3 days. The crystals were collected, washed with water (50 ml) and then ether (50 ml), and dried at 35° for 16 hours in vacuo to give 10.94 g of desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723609
출처 데이터셋uspto-grants-1998_03
ORD IDord-63652823dab044f195e03b0122ca1c8d
출처 메모uspto-grants-1998_03